22488-76-2

Basic information

• Product Name: 3-(2-FURYL)-1-PHENYL-2-PROPEN-1-ONE
• Synonyms: 3-(2-FURYL)-1-PHENYL-2-PROPEN-1-ONE;(2Z)-3-(furan-2-yl)-1-phenylprop-2-en-1-one
• CAS NO: 22488-76-2
• Molecular Formula: C₁₃H₁₀O₂
• Molecular Weight: 198.22
• Mol File: 22488-76-2.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-(2-FURYL)-1-PHENYL-2-PROPEN-1-ONE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(2-FURYL)-1-PHENYL-2-PROPEN-1-ONE(22488-76-2)
• EPA Substance Registry System: 3-(2-FURYL)-1-PHENYL-2-PROPEN-1-ONE(22488-76-2)

Safety Data

• Hazardous Substances Data: 22488-76-2(Hazardous Substances Data)

Upstream product

• 39511-12-1 (E)-3-(furan-2-yl)-1-phenyl-2-propen-1-one 
• 98-01-1 furfural 
• 2648-61-5 2,2-dichloroacetophenone 

Relevant articles and documents

Synthesis of E-α,β-unsaturated ketones with complete stereoselectivity via sequential aldol-type/elimination reactions promoted by samarium diiodide or chromium dichloride

E-α,β-Unsaturated ketones can be obtained with complete E-selectivity by a sequential reaction of dichloroketones with a variety of aldehydes. This transformation was promoted by SmI2, SmI2 in the presence of FeCl3 or CrCl2. The best results were obtained when CrCl2 was used as the metallating agent. A mechanism based on a successive aldol-type reaction and a β-elimination is proposed to explain these results. Georg Thieme Verlag Stuttgart.